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Transcription Regulation of ompF and ompC by a Single Transcription Factor, OmpR

The Journal of biological chemistry, 2006-06, Vol.281 (25), p.17114-17123

2006

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Cyclopentane-based human NK1 antagonists. Part 2: Development of potent, orally active, water-soluble derivatives

Bioorganic & medicinal chemistry letters, 2006-09, Vol.16 (17), p.4504-4511

2006

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Signal transduction via the histidyl‐aspartyl phosphorelay

Genes to cells : devoted to molecular & cellular mechanisms, 1997-03, Vol.2 (3), p.167-184

1997

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Bioisosteric replacement of anilide with benzoxazole: potent and orally bioavailable antagonists of VLA-4

Bioorganic & medicinal chemistry letters, 2004-05, Vol.14 (9), p.2331-2334

2004

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Nucleoside-diphosphate Kinase-mediated Signal Transduction via Histidyl-Aspartyl Phosphorelay Systems in Escherichia coli

The Journal of biological chemistry, 1996-12, Vol.271 (51), p.32886-32893

1996

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N-Tetrahydrofuroyl-( l)-phenylalanine derivatives as potent VLA-4 antagonists

Bioorganic & medicinal chemistry letters, 2002-06, Vol.12 (11), p.1497-1500

2002

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Specific and dual antagonists of α4β1 and α4β7 integrins

Bioorganic & medicinal chemistry letters, 2002-01, Vol.12 (2), p.133-136

2002

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The discovery of small molecule carbamates as potent dual α4β1/α4β7 integrin antagonists

Bioorganic & medicinal chemistry letters, 2002-01, Vol.12 (2), p.159-163

2002

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Substituted tetrahydrofuroyl-1-phenylalanine derivatives as potent and specific VLA-4 antagonists

Bioorganic & medicinal chemistry letters, 2002-06, Vol.12 (11), p.1501-1505

2002

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N-(3-Phenylsulfonyl-3-piperidinoyl)-phenylalanine derivatives as potent, selective VLA-4 antagonists

Bioorganic & medicinal chemistry letters, 2003-03, Vol.13 (5), p.885-890

2003

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N-Aryl-prolyl-dipeptides as potent antagonists of VLA-4

Bioorganic & medicinal chemistry letters, 2002-08, Vol.12 (16), p.2205-2208

2002

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Substituted 3-amino biaryl propionic acids as potent VLA-4 antagonists

Bioorganic & medicinal chemistry letters, 2002-09, Vol.12 (17), p.2415-2418

2002

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The Discovery of acylated β-Amino acids as potent and orally bioavailable VLA-4 antagonists

Bioorganic & medicinal chemistry letters, 2002-02, Vol.12 (4), p.611-614

2002

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IL-1 beta-converting enzyme is present in monocytic cells as an inactive 45-kDa precursor

The Journal of immunology (1950), 1994-09, Vol.153 (6), p.2592-2599

1994

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Purification and Characterization of the Periplasmic Domain of EnvZ Osmosensor inEscherichia coli

Biochemical and biophysical research communications, 1997-02, Vol.231 (1), p.68-72

1997

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Specific and dual antagonists of alpha(4)beta(1) and alpha(4)beta(7) integrins

Bioorganic & medicinal chemistry letters, 2002-01, Vol.12 (2), p.133-136

2002

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Purification and characterization of active human interleukin-1 beta-converting enzyme from THP.1 monocytic cells

The Journal of biological chemistry, 1993-08, Vol.268 (24), p.18062-18069

1993

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The discovery of small molecule carbamates as potent dual alpha(4)beta(1)/alpha(4)beta(7) integrin antagonists

Bioorganic & medicinal chemistry letters, 2002-01, Vol.12 (2), p.159-163

2002

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Hierarchical and co‐operative binding of OmpR to a fusion construct containing the ompC and ompF upstream regulatory sequences of Escherichia coli

Genes to cells : devoted to molecular & cellular mechanisms, 1998-12, Vol.3 (12), p.777-788

1998

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Purification and characterization of the periplasmic domain of EnvZ osmosensor in Escherichia coli

Biochemical and biophysical research communications, 1997-02, Vol.231 (1), p.68-72

1997

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Alpha(4)beta(7)/alpha(4)beta(1) dual integrin antagonists block alpha(4)beta(7)-dependent adhesion under shear flow

The Journal of pharmacology and experimental therapeutics, 2002-07, Vol.302 (1), p.153

2002

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A small molecule alpha4beta1/alpha4beta7 antagonist differentiates between the low-affinity states of alpha4beta1 and alpha4beta7: characterization of divalent cation dependence

The Journal of pharmacology and experimental therapeutics, 2003-09, Vol.306 (3), p.903

2003

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A Small Molecule α 4 β 1 /α 4 β 7 Antagonist Differentiates between the Low-Affinity States of α 4 β 1 and α 4 β 7 : Characterization of Divalent Cation Dependence

The Journal of pharmacology and experimental therapeutics, 2003-09, Vol.306 (3), p.903-913

2003

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Specific and dual antagonists of α 4β 1 and α 4β 7 integrins

Bioorganic & medicinal chemistry letters, 2002, Vol.12 (2), p.133-136

2002

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The discovery of small molecule carbamates as potent dual α 4β 1/α 4β 7 integrin antagonists

Bioorganic & medicinal chemistry letters, 2002, Vol.12 (2), p.159-163

2002

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Transcription Regulation of ompF and ompC by a Single Transcription Factor, OmpR

Cyclopentane-based human NK1 antagonists. Part 2: Development of potent, orally active, water-soluble derivatives

Signal transduction via the histidyl‐aspartyl phosphorelay

Bioisosteric replacement of anilide with benzoxazole: potent and orally bioavailable antagonists of VLA-4

Nucleoside-diphosphate Kinase-mediated Signal Transduction via Histidyl-Aspartyl Phosphorelay Systems in Escherichia coli

N-Tetrahydrofuroyl-( l)-phenylalanine derivatives as potent VLA-4 antagonists

Specific and dual antagonists of α4β1 and α4β7 integrins

The discovery of small molecule carbamates as potent dual α4β1/α4β7 integrin antagonists

Substituted tetrahydrofuroyl-1-phenylalanine derivatives as potent and specific VLA-4 antagonists

N-(3-Phenylsulfonyl-3-piperidinoyl)-phenylalanine derivatives as potent, selective VLA-4 antagonists

N-Aryl-prolyl-dipeptides as potent antagonists of VLA-4

Substituted 3-amino biaryl propionic acids as potent VLA-4 antagonists

The Discovery of acylated β-Amino acids as potent and orally bioavailable VLA-4 antagonists

IL-1 beta-converting enzyme is present in monocytic cells as an inactive 45-kDa precursor

Purification and Characterization of the Periplasmic Domain of EnvZ Osmosensor inEscherichia coli

Specific and dual antagonists of alpha(4)beta(1) and alpha(4)beta(7) integrins

Purification and characterization of active human interleukin-1 beta-converting enzyme from THP.1 monocytic cells

The discovery of small molecule carbamates as potent dual alpha(4)beta(1)/alpha(4)beta(7) integrin antagonists

Hierarchical and co‐operative binding of OmpR to a fusion construct containing the ompC and ompF upstream regulatory sequences of Escherichia coli

Purification and characterization of the periplasmic domain of EnvZ osmosensor in Escherichia coli

Alpha(4)beta(7)/alpha(4)beta(1) dual integrin antagonists block alpha(4)beta(7)-dependent adhesion under shear flow

A small molecule alpha4beta1/alpha4beta7 antagonist differentiates between the low-affinity states of alpha4beta1 and alpha4beta7: characterization of divalent cation dependence

A Small Molecule α 4 β 1 /α 4 β 7 Antagonist Differentiates between the Low-Affinity States of α 4 β 1 and α 4 β 7 : Characterization of Divalent Cation Dependence

Specific and dual antagonists of α 4β 1 and α 4β 7 integrins

The discovery of small molecule carbamates as potent dual α 4β 1/α 4β 7 integrin antagonists

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